Singleton AB - Search Results

1

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

Höglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, Hurtig HI, Gross RG, Maetzler W, Goldwurm S, Tolosa E, Borroni B, Pastor P; PSP Genetics Study Group; Cantwell LB, Han MR, Dillman A, van der Brug MP, Gibbs JR, Cookson MR, Hernandez DG, Singleton AB, Farrer MJ, Yu CE, Golbe LI, Revesz T, Hardy J, Lees AJ, Devlin B, Hakonarson H, Müller U, Schellenberg GD. Höglinger GU, et al. Among authors: singleton ab. Nat Genet. 2011 Jun 19;43(7):699-705. doi: 10.1038/ng.859. Nat Genet. 2011. PMID: 21685912 Free PMC article.

2

Normal localization of deltaF323-Y328 mutant torsinA in transfected human cells.

O'Farrell C, Hernandez DG, Evey C, Singleton AB, Cookson MR. O'Farrell C, et al. Among authors: singleton ab. Neurosci Lett. 2002 Jul 19;327(2):75-8. doi: 10.1016/s0304-3940(02)00400-7. Neurosci Lett. 2002. PMID: 12098639

3

Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease.

Goudreau JL, Maraganore DM, Farrer MJ, Lesnick TG, Singleton AB, Bower JH, Hardy JA, Rocca WA. Goudreau JL, et al. Among authors: singleton ab. Mov Disord. 2002 Nov;17(6):1305-11. doi: 10.1002/mds.10268. Mov Disord. 2002. PMID: 12465073

4

Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis.

Garcia ML, Singleton AB, Hernandez D, Ward CM, Evey C, Sapp PA, Hardy J, Brown RH Jr, Cleveland DW. Garcia ML, et al. Among authors: singleton ab. Neurobiol Dis. 2006 Jan;21(1):102-9. doi: 10.1016/j.nbd.2005.06.016. Epub 2005 Aug 3. Neurobiol Dis. 2006. PMID: 16084104

5

Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Lee-Chen GJ, Wu YR. Fung HC, et al. Among authors: singleton ab. Neurosci Lett. 2006 Feb 6;394(1):33-6. doi: 10.1016/j.neulet.2005.10.005. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257123

6

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Wu YR. Fung HC, et al. Among authors: singleton ab. BMC Neurol. 2006 Dec 22;6:47. doi: 10.1186/1471-2377-6-47. BMC Neurol. 2006. PMID: 17187665 Free PMC article.

7

Clinical heterogeneity of ATP13A2 linked disease (Kufor-Rakeb) justifies a PARK designation.

Lees AJ, Singleton AB. Lees AJ, et al. Among authors: singleton ab. Neurology. 2007 May 8;68(19):1553-4. doi: 10.1212/01.wnl.0000265228.66664.f4. Neurology. 2007. PMID: 17485640 No abstract available.

8

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.

Houlden H, Johnson J, Gardner-Thorpe C, Lashley T, Hernandez D, Worth P, Singleton AB, Hilton DA, Holton J, Revesz T, Davis MB, Giunti P, Wood NW. Houlden H, et al. Among authors: singleton ab. Nat Genet. 2007 Dec;39(12):1434-6. doi: 10.1038/ng.2007.43. Epub 2007 Nov 25. Nat Genet. 2007. PMID: 18037885

9

Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls.

Paisán-Ruíz C, Nath P, Washecka N, Gibbs JR, Singleton AB. Paisán-Ruíz C, et al. Among authors: singleton ab. Hum Mutat. 2008 Apr;29(4):485-90. doi: 10.1002/humu.20668. Hum Mutat. 2008. PMID: 18213618

10

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.

Camargos S, Scholz S, Simón-Sánchez J, Paisán-Ruiz C, Lewis P, Hernandez D, Ding J, Gibbs JR, Cookson MR, Bras J, Guerreiro R, Oliveira CR, Lees A, Hardy J, Cardoso F, Singleton AB. Camargos S, et al. Among authors: singleton ab. Lancet Neurol. 2008 Mar;7(3):207-15. doi: 10.1016/S1474-4422(08)70022-X. Epub 2008 Feb 1. Lancet Neurol. 2008. PMID: 18243799

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